US4479985A - Method for cleaning and clearing plastic surfaces - Google Patents
Method for cleaning and clearing plastic surfaces Download PDFInfo
- Publication number
- US4479985A US4479985A US06/331,489 US33148981A US4479985A US 4479985 A US4479985 A US 4479985A US 33148981 A US33148981 A US 33148981A US 4479985 A US4479985 A US 4479985A
- Authority
- US
- United States
- Prior art keywords
- formulation
- cleaning
- resin
- coating
- alkyd
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/0427—Coating with only one layer of a composition containing a polymer binder
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/043—Improving the adhesiveness of the coatings per se, e.g. forming primers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2333/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2333/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
- C08J2333/06—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C08J2333/10—Homopolymers or copolymers of methacrylic acid esters
- C08J2333/12—Homopolymers or copolymers of methyl methacrylate
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31909—Next to second addition polymer from unsaturated monomers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31909—Next to second addition polymer from unsaturated monomers
- Y10T428/31924—Including polyene monomers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31909—Next to second addition polymer from unsaturated monomers
- Y10T428/31928—Ester, halide or nitrile of addition polymer
Definitions
- This invention relates to a method and composition for cleaning and preserving in a clear condition transparent plastic sheets for example, windows, such as "PLEXIGLAS".
- U.S. Pat. Nos. 3,904,732 and 3,677,821 are broadly directed to restoring the surfaces of plastic sheets such as "LUCITE” and “PLEXIGLAS", polymethylmethacrylates.
- My invention is more particularly directed to overcoming the problems associated with so-called plastic or synthetic transparent windows such as those windows formulated primarily or entirely from methylmethacrylate.
- my invention comprises cleaning a surface of a transparent methylmethacrylate (a thermoplastic poly-type polymer more specifically an acrylic monomer).
- a transparent methylmethacrylate a thermoplastic poly-type polymer more specifically an acrylic monomer.
- the first step comprises cleaning the surface to remove the opacity and subsequently coating the cleaned surface to prevent further clouding.
- a composition of a petroleum distillate emulsified in water is suitable.
- the petroleum distillate is a mixture of hydrocarbons having a boiling point between 150°-190° C.; that is, the fraction in the distillation of petroleum between gasoline and the fuel oils as determined in accordance with Standard Method of Tests for Distillation of Gasoline, Naptha, Kerosene and Similar Petroleum Products (ASTM D 86).
- the petroleum products found in this range are typically referred to as kerosene, coal oil, astrol oil or, more broadly, paraffinic mixtures of hydrocarbons as identified by their boiling point ranges.
- paraffinic hydrocarbons may be applied directly in the cleaning step or may be emulsified with water of up to one part hydrocarbon to nine parts water by volume.
- a pine oil-alcohol-water composition may be used such as Pine-Sol a product of American Cyanamid.
- the coating composition comprises a polyester resin, such as an alkyd resin.
- the alkyd resin is modified with an oil such as linseed, safflower, tung, and soy bean, and is further modified or copolymerized with monomers such as urethane, vinyl toluene, acrylic and/or vinyl monomers.
- the resin is dissolved in a solvent such as petroleum distillates having a boiling point range of between 150° to 190° C. such as mineral spirits and optionally dryers are added which would be compatible with the formulation.
- the dryers are any compatible oxidant which hastens the drying of the composition, such as a solution of lead, manganese or zinc salts of resin acids.
- My invention will be described in reference to the cleaning and coating of surfaces of transparent acrylic windows, or sheets, the surfaces of which have become cloudy due to exposure to the sun.
- a transparent acrylic sheet as commercially available is sold under the trademarks LUCITE or PLEXIGLAS, both well-known polymethylmethacrylates and products of DuPont and Rohm & Hass, respectively.
- the cleaning step to clear the surfaces was accomplished as follows.
- An aqueous emulsion of a petroleum distillate was used.
- the petroleum distillate used is available commercially as kerosene. When emulsified in water, it is commercially sold under the trademark LESTOIL.
- the cleaning solution was applied to the clouded surface by rubbing the mixture on the clouded surface, preferably using a circular motion. After rubbing for a predetermined time, between about 10 seconds to 1 minute, for example 30 seconds the surface was cleared and was subsequently wiped dry. At this point, the surface appeared to be transparent but the surface reclouded within an hour or more. Generally the clouded surface is the surface exposed directly to the sunlight. Depending upon the location and use of the sheet only one surface or both surfaces may have to be cleaned and coated.
- the coating was applied by spraying it with a commercial sprayer preferably starting at the top of the sheet with the window standing in an upright position and allowing the material to drain down. The coating was continuously applied until no ripples appear and a uniform film is formed. The coating was then is allowed to air dry.
- the coating is a hard clear gloss coating with excellent adhesion, abrasion resistance, good weathering, excellent chemical resistance and flexibility.
- the oil modified-alkyd resins are combined with a monomer, for example, stryene, urethane, vinyl toluene, or acrylic monomers. Urethane alkyd is preferred.
- LESTOIL For the cleaning solution, the commercial formulation of LESTOIL was used with varying amounts of water. More specifically, in parts by volume, LESTOIL/water the following ratios were found satisfactory: 1:0.5; 1:1; 1:2 and 1:3 to completely clear the surface.
- PINE SOL having the formulation; Pine oil 30.0%; isopropanol 10.9%; soap 10%; and water 49.1% was used.
- any solvent such as mineral spirits which would be a volatile component compatible with the formulation may be used.
- mineral spirits having a bulking value of 6.50 lbs. per gallon the percent volatile by weight in the final formulation based on the addition of 12-20 fluid ozs. will range between about 71 to 78%. This is based on the additional between 12 and 20 fluid ozs. of solvent, such as mineral spirits to the commercially available formulations described above.
- the dryers may be added optionally, as desired.
- the formulations may be used alone to both clean and coat the surfaces.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Detergent Compositions (AREA)
Abstract
Clouded acrylate surfaces are cleaned permanently. The clouded surface is first cleaned using a petroleum distillate. Subsequently, a coating of an oil-monomer modified alkyl resin, 71-78% non-volatile, is coated on the surface to prevent further clouding.
Description
This application is a continuation of application Ser. No. 973,400, filed Dec. 26, 1978 now abandoned.
This invention relates to a method and composition for cleaning and preserving in a clear condition transparent plastic sheets for example, windows, such as "PLEXIGLAS".
U.S. Pat. Nos. 3,904,732 and 3,677,821 are broadly directed to restoring the surfaces of plastic sheets such as "LUCITE" and "PLEXIGLAS", polymethylmethacrylates.
My invention is more particularly directed to overcoming the problems associated with so-called plastic or synthetic transparent windows such as those windows formulated primarily or entirely from methylmethacrylate.
These windows after a period of time tend to cloud or become less transparent and therefore more opaque. In the cleaning of these windows with the use of commercial cleaners, two problems have been encountered: first, most commercial cleaners, such as are available to consumers at the retail level, will not remove the cloudiness or opaqueness from these windows; second, those few commercial cleaners available that will, in fact, clear the windows, such as "LESTOIL"®, a product of Noxell Corporation of Baltimore, Md., will only temporarily restore the transparency.
I have overcome the aforementioned problems of the inability to clean and maintain such windows in a clear or transparent condition by using a two-step process to clear permanently such windows. If the windows are initially clear, then only one of the two steps of my process and formulation is required.
Broadly, my invention comprises cleaning a surface of a transparent methylmethacrylate (a thermoplastic poly-type polymer more specifically an acrylic monomer). Where the acrylic surface is clouded, the first step comprises cleaning the surface to remove the opacity and subsequently coating the cleaned surface to prevent further clouding.
In the first step it has been found that a composition of a petroleum distillate emulsified in water is suitable. The petroleum distillate is a mixture of hydrocarbons having a boiling point between 150°-190° C.; that is, the fraction in the distillation of petroleum between gasoline and the fuel oils as determined in accordance with Standard Method of Tests for Distillation of Gasoline, Naptha, Kerosene and Similar Petroleum Products (ASTM D 86). The petroleum products found in this range are typically referred to as kerosene, coal oil, astrol oil or, more broadly, paraffinic mixtures of hydrocarbons as identified by their boiling point ranges. These paraffinic hydrocarbons may be applied directly in the cleaning step or may be emulsified with water of up to one part hydrocarbon to nine parts water by volume. Alternatively a pine oil-alcohol-water composition may be used such as Pine-Sol a product of American Cyanamid.
In the second step of the process, a coating composition is applied. The coating composition forms a film which permanently adheres to the surface and prevents further clouding. Also, it has been found that the formulations per se will clean the surface but not to the same degree of clearness (clarity) as the combination of both steps. Broadly, the coating composition comprises a polyester resin, such as an alkyd resin. The alkyd resin is modified with an oil such as linseed, safflower, tung, and soy bean, and is further modified or copolymerized with monomers such as urethane, vinyl toluene, acrylic and/or vinyl monomers. The resin is dissolved in a solvent such as petroleum distillates having a boiling point range of between 150° to 190° C. such as mineral spirits and optionally dryers are added which would be compatible with the formulation. The dryers are any compatible oxidant which hastens the drying of the composition, such as a solution of lead, manganese or zinc salts of resin acids.
My invention will be described in reference to the cleaning and coating of surfaces of transparent acrylic windows, or sheets, the surfaces of which have become cloudy due to exposure to the sun.
A transparent acrylic sheet as commercially available is sold under the trademarks LUCITE or PLEXIGLAS, both well-known polymethylmethacrylates and products of DuPont and Rohm & Hass, respectively.
The surfaces of such sheets after a period of time, as is well known, tend to cloud or become opaque rendering the window less transparent. In order to clean permanently the sheet the following steps are effected.
In the following Examples the cleaning step to clear the surfaces was accomplished as follows. An aqueous emulsion of a petroleum distillate was used. The petroleum distillate used is available commercially as kerosene. When emulsified in water, it is commercially sold under the trademark LESTOIL. The cleaning solution was applied to the clouded surface by rubbing the mixture on the clouded surface, preferably using a circular motion. After rubbing for a predetermined time, between about 10 seconds to 1 minute, for example 30 seconds the surface was cleared and was subsequently wiped dry. At this point, the surface appeared to be transparent but the surface reclouded within an hour or more. Generally the clouded surface is the surface exposed directly to the sunlight. Depending upon the location and use of the sheet only one surface or both surfaces may have to be cleaned and coated.
In the following Examples, the coating was applied by spraying it with a commercial sprayer preferably starting at the top of the sheet with the window standing in an upright position and allowing the material to drain down. The coating was continuously applied until no ripples appear and a uniform film is formed. The coating was then is allowed to air dry.
The coating is a hard clear gloss coating with excellent adhesion, abrasion resistance, good weathering, excellent chemical resistance and flexibility. The oil modified-alkyd resins are combined with a monomer, for example, stryene, urethane, vinyl toluene, or acrylic monomers. Urethane alkyd is preferred.
For the cleaning solution, the commercial formulation of LESTOIL was used with varying amounts of water. More specifically, in parts by volume, LESTOIL/water the following ratios were found satisfactory: 1:0.5; 1:1; 1:2 and 1:3 to completely clear the surface.
Alternatively for the cleaning solution, PINE SOL having the formulation; Pine oil 30.0%; isopropanol 10.9%; soap 10%; and water 49.1% was used.
U2 polyurethane-Clear Gloss as manufactured by Sterling Clark Lurton Corporation, Malden, Mass., having the formulation by weight percent linseed alkyd modified with toluene diisocyanate, 45% and mineral spirits and dryers 55% was used. To 32 fluid ozs. of this commercial coating was added 16 fluid ozs. of mineral spirits and 1 fluid oz. of dryers. The final formulation was applied to the cleaned surface before reclouding commenced, e.g., within 10 to 20 minutes. Three months after coating, the window remained transparent.
A Polyurethane Varnish 012 Gloss Spar as manufactured by General Paint and Chemical Company, Division of Cotter & Company, Chicago, Ill., having the formulation by weight percent, non-volatile 41% (toluene dissocyanate soya copolymer), volatile 59% (mineral spirits 99%, dryers 1%) was used. To 32 fluid ozs. of this commercial coating as in Example I, was added 16 fluid ozs. of mineral spirits and 1 fluid oz. of dryers. A cleaned surface was coated with formulation before reclouding commenced. After three months the window was still transparent.
70-28 (568) Semi-Gloss as manufactured by Dutchboy Paints, West Caldwell, N.J., having the formulation by weight percent, non-volatile (vinyl alkyd copolymer) 33.7% and volatile (mineral spirits) 66.3% was used. To 32 fluid ozs. of this commercial coating was added 16 fluid ozs of mineral spirits and 1.0 fluid oz. of dryers. A cleared surface was coated with this formulation. After three months the window was still transparent.
For all surfaces cleaned but not coated re-clouding commenced within one hour.
Although 16 fluid ozs. of mineral spirits was used, any solvent such as mineral spirits which would be a volatile component compatible with the formulation, may be used. Where mineral spirits are used having a bulking value of 6.50 lbs. per gallon the percent volatile by weight in the final formulation based on the addition of 12-20 fluid ozs. will range between about 71 to 78%. This is based on the additional between 12 and 20 fluid ozs. of solvent, such as mineral spirits to the commercially available formulations described above. The dryers may be added optionally, as desired.
Depending on the degree of clouding the formulations may be used alone to both clean and coat the surfaces.
Claims (7)
1. A method for cleaning and preventing clouding of transparent methylmethacrylate sheets which includes:
coating the surface of the sheet with a formulation which consists essentially of a non-volatile oil-monomer modified alkyd resin, the monomer selected from the group consisting of styrene, vinyl toluene, urethane and acrylic monomers; and a volatile solvent, the solvent being a petroleum distillate having a boiling point range between 150°-190° C., the non-volatile resin comprising 22-29% by weight of the formulation and the volume volatile solvent comprising 78-71% by weight of the formulation to form a clear film which prevents clouding of the acrylate sheet.
2. The method of claim 1 wherein the oil is selected from the group consisting of linseed, safflower, tung and soybean oils.
3. The method of claim 1 wherein the resin is linseed alkyd modified with toluene diisocyante.
4. The method of claim 1 wherein the resin is soya alkyd modified with toluene diisocyante.
5. The method of claim 1 wherein the resin is modified with a vinyl alkyd copolymer.
6. The method of claims 1, 2, 3, 4 or 5 which includes:
cleaning the acrylate surface with a petroleum distillate having a boiling point range of between 150°-180° prior to coating the surface.
7. The method of claims 1, 2, 3, 4 or 5 which includes:
cleaning the acrylate surface with a pine oil-alcohol-water formulation.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/331,489 US4479985A (en) | 1978-12-26 | 1981-12-17 | Method for cleaning and clearing plastic surfaces |
US06/666,563 US4595719A (en) | 1981-12-17 | 1984-10-30 | Composition for cleaning and clearing plastic surfaces |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US97340078A | 1978-12-26 | 1978-12-26 | |
US06/331,489 US4479985A (en) | 1978-12-26 | 1981-12-17 | Method for cleaning and clearing plastic surfaces |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US97340078A Continuation | 1978-12-26 | 1978-12-26 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US06/666,563 Division US4595719A (en) | 1981-12-17 | 1984-10-30 | Composition for cleaning and clearing plastic surfaces |
Publications (1)
Publication Number | Publication Date |
---|---|
US4479985A true US4479985A (en) | 1984-10-30 |
Family
ID=26987786
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US06/331,489 Expired - Fee Related US4479985A (en) | 1978-12-26 | 1981-12-17 | Method for cleaning and clearing plastic surfaces |
Country Status (1)
Country | Link |
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US (1) | US4479985A (en) |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1643251A (en) * | 1926-08-11 | 1927-09-20 | George A Mcbride | Composition for cleaning and polishing glass |
US1764392A (en) * | 1925-04-29 | 1930-06-17 | Diebold Fritz | Composition for cleaning glass windows |
US1875552A (en) * | 1929-10-28 | 1932-09-06 | Goodyear Tire & Rubber | Mold cleaning solution |
US2713039A (en) * | 1948-06-22 | 1955-07-12 | American Cyanamid Co | Modified alkyd resins and process of preparing same |
US2862898A (en) * | 1954-10-07 | 1958-12-02 | Monsanto Chemcial Company | Modified alkyd resins |
US2967163A (en) * | 1959-03-25 | 1961-01-03 | Jacob M Fain | Rain repellent composition comprising a styrenated oil modified alkyd resin with paraffin wax |
US2986543A (en) * | 1958-10-20 | 1961-05-30 | American Cyanamid Co | Process for preparing styrenated nondrying and/or semi-drying oil modified alkyd resins by incremental monomeric addition |
US3382294A (en) * | 1963-05-03 | 1968-05-07 | Pittsburgh Plate Glass Co | Coating composition comprising an acrylic inter-polymer, an amine-aldehyde resin, and an alkyd resin |
US3501425A (en) * | 1964-07-30 | 1970-03-17 | Reichhold Chemicals Inc | Process for preparing thixotropic solutions of oil-modified alkyd resins and resulting product |
US3515579A (en) * | 1968-06-21 | 1970-06-02 | Nat Patent Dev Corp | Non-fogging transparent material |
US3677821A (en) * | 1967-12-29 | 1972-07-18 | Lion Fat Oil Co Ltd | Method for reconditioning the surface of plastics |
US3876575A (en) * | 1970-07-22 | 1975-04-08 | Nippon Oil Co Ltd | Process for producing resins of weather resistance |
US3904732A (en) * | 1974-10-22 | 1975-09-09 | Us Army | Method for improving transparency of thermally damaged acrylic glazing |
-
1981
- 1981-12-17 US US06/331,489 patent/US4479985A/en not_active Expired - Fee Related
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1764392A (en) * | 1925-04-29 | 1930-06-17 | Diebold Fritz | Composition for cleaning glass windows |
US1643251A (en) * | 1926-08-11 | 1927-09-20 | George A Mcbride | Composition for cleaning and polishing glass |
US1875552A (en) * | 1929-10-28 | 1932-09-06 | Goodyear Tire & Rubber | Mold cleaning solution |
US2713039A (en) * | 1948-06-22 | 1955-07-12 | American Cyanamid Co | Modified alkyd resins and process of preparing same |
US2862898A (en) * | 1954-10-07 | 1958-12-02 | Monsanto Chemcial Company | Modified alkyd resins |
US2986543A (en) * | 1958-10-20 | 1961-05-30 | American Cyanamid Co | Process for preparing styrenated nondrying and/or semi-drying oil modified alkyd resins by incremental monomeric addition |
US2967163A (en) * | 1959-03-25 | 1961-01-03 | Jacob M Fain | Rain repellent composition comprising a styrenated oil modified alkyd resin with paraffin wax |
US3382294A (en) * | 1963-05-03 | 1968-05-07 | Pittsburgh Plate Glass Co | Coating composition comprising an acrylic inter-polymer, an amine-aldehyde resin, and an alkyd resin |
US3501425A (en) * | 1964-07-30 | 1970-03-17 | Reichhold Chemicals Inc | Process for preparing thixotropic solutions of oil-modified alkyd resins and resulting product |
US3677821A (en) * | 1967-12-29 | 1972-07-18 | Lion Fat Oil Co Ltd | Method for reconditioning the surface of plastics |
US3515579A (en) * | 1968-06-21 | 1970-06-02 | Nat Patent Dev Corp | Non-fogging transparent material |
US3876575A (en) * | 1970-07-22 | 1975-04-08 | Nippon Oil Co Ltd | Process for producing resins of weather resistance |
US3904732A (en) * | 1974-10-22 | 1975-09-09 | Us Army | Method for improving transparency of thermally damaged acrylic glazing |
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